PR

Product NDC: 72358-101
11-digit product format: 723580101
Labeler code: 72358
Product ID: 72358-101_4229f4ae-8934-0e10-e063-6394a90a4185
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: LOTION
Route: TOPICAL
Labeler: Amphp, Inc
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-11-01
Substance: MENTHOL
Active strength: .5 g/100g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 9 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72358-101-04	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72358-101-03	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72358-101-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72358-101-03	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72358-101-04	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72358-101-03	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: PR
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	.5 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1293193	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
6f5b9e08-c445-4fac-e053-2a91aa0aa737	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72358-101-03	2025-03-03	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2025-03-03	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-04	2025-03-03	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-04	2025-03-03	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2025-01-30	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2025-01-30	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-04	2025-01-30	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-04	2025-01-30	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-01	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-01	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-02	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-02	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-01	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-01	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-02	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-02	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72358-101-03	PR	20 g in 1 PACKET	LOTION	20		9
72358-101-04	PR	300 g in 1 BOTTLE, PLASTIC	LOTION	300		9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72358-101	PR (MENTHOL) LOTION [AMPHP, INC]	8	Current NDC, Legacy NDC, 2 package rows	20250305_6f5b9e08-c445-4fac-e053-2a91aa0aa737.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 67 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
QIAN LI ZHUI FENG PAIN RELIEVING	CAMPHOR, MENTHOL, AND METHYL SALICYLATE	MADISON ONE ACME INC	03a4fb7c-2328-409d-99c8-cbcf2b4a451f	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
WU YANG BRAND PAIN RELIEVING MEDICATED	MENTHOL AND CAMPHOR	MADISON ONE ACME INC	05c6b95a-aeb6-4234-97c7-8d77eccb38d8	2025-11-10	Warnings	Exact identifier application number: M017
HEI GUI PAIN RELIEVING	CAMPHOR AND METHYL SALICYLATE	MADISON ONE ACME INC	4140c404-edab-4923-941d-f74125e943a9	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
E MEI SHAN MEDICATED	CAMPHOR AND MENTHOL	MADISON ONE ACME INC	ddcc814e-fcc4-4232-9ab4-826b8aac35f0	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
Overtime	METHYL SALICYLATE, MENTHOL AND CAPSAICIN	Physicians Science & Nature Inc.	25fec070-8587-42d1-ba6f-1a9c150acc98	2025-11-10	Warnings	Exact identifier application number: M017
Dendracin Neurodendraxcin	METHYL SALICYLATE, MENTHOL AND CAPSAICIN	Physicians Science & Nature Inc.	05742cd5-ece2-4007-bdf0-46b76d23df74	2025-11-10	Warnings	Exact identifier application number: M017
Anal Blu	DESENSITIZER	Novelties by Nasswalk, Inc.	03b9555b-c3ff-4baa-e063-6394a90afb2c	2025-11-10	Warnings	Exact identifier application number: M017
Stallion	DELAY CREME	Novelties by Nasswalk, Inc.	0261ec88-8fe4-d5f8-e063-6294a90ab3d4	2025-11-10	Warnings	Exact identifier application number: M017
ANAL-ESE	DESENSITIZER	Novelties by Nasswalk, Inc.	03b89eed-b433-a263-e063-6294a90a675b	2025-11-10	Warnings	Exact identifier application number: M017
Instant Erection	ULTIMATE ERECTION ENHANCER	Novelties by Nasswalk, Inc.	03a444f9-7052-0c38-e063-6294a90a4e56	2025-11-10	Warnings	Exact identifier application number: M017
STA-HARD	DESENSITIZING LUBRICANT	Novelties by Nasswalk, Inc.	02ef794b-8e70-5c26-e063-6294a90a28d1	2025-11-10	Warnings	Exact identifier application number: M017
ANAL-ESE	DESENSITIZER	Novelties by Nasswalk, Inc.	03a4a7ce-4cff-a608-e063-6294a90ad65d	2025-11-10	Warnings	Exact identifier application number: M017
FOOTSPA PEDI	ALCOHOL	CHEMCO CORPORATION	04de4392-74f6-7df8-e063-6294a90ae3b1	2025-11-08	Warnings	Exact identifier application number: M017
Johnson and Johnson All Purpose First Aid Kit	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	5cdb47c5-7951-4279-8a05-0a3199d3dd45	2025-11-06	Warnings	Exact identifier application number: M017
Johnson and Johnson First Aid Travel Ready 80 CT	ACETAMINOPHEN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	f388f105-48ba-4616-e053-2a95a90a0049	2025-11-06	Warnings	Exact identifier application number: M017
Johnson and Johnson First Aid All Purpose 160 CT	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	f3933330-2550-4a88-e053-2a95a90a3997	2025-11-06	Warnings	Exact identifier application number: M017
Foot and Leg Pain Relief	LIDOCAINE	Premier Brands of America Inc.	42f23e2f-11c6-da49-e063-6294a90ac720	2025-11-06	Warnings	Exact identifier application number: M017
HEALING TREE CALMING ANTI-ITCH	HYDROCORTISONE	Renu Laboratories, LLC	fc8bcde9-26e8-a35f-e053-6394a90a3300	2025-11-06	Warnings	Exact identifier application number: M017
Calamine Plus	CALAMINE PLUS PRAMOXINE HCL	Chain Drug Marketing Association Inc	1a3f8819-58cf-8923-e063-6394a90a37af	2025-11-06	Warnings	Exact identifier application number: M017
Extra Strength Itch Relief	DIPHENHYDRAMINE HCL AND ZINC ACETATE	Chain Drug Marketing Association Inc	1a2997bc-7741-e658-e063-6394a90af6fd	2025-11-06	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1293193	menthol 0.5 % Topical Lotion	PSN	6f5b9e08-c445-4fac-e053-2a91aa0aa737	9
1293193	menthol 5 MG/ML Topical Lotion	SCD	6f5b9e08-c445-4fac-e053-2a91aa0aa737	9
1293193	menthol 0.5 % Topical Lotion	SY	6f5b9e08-c445-4fac-e053-2a91aa0aa737	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72358-101-01	72358010101	300 g in 1 TUBE (72358-101-01)	300 g	2018-11-01	0000-00-00	No	No	Current
72358-101-02	72358010102	100 g in 1 TUBE (72358-101-02)	100 g	2018-11-01	0000-00-00	No	No	Current
72358-101-03	72358010103	20 g in 1 PACKET (72358-101-03)	20 g	2018-11-01	0000-00-00	No	No	Current
72358-101-04	72358010104	300 g in 1 BOTTLE, PLASTIC (72358-101-04)	300 g	2018-11-01	0000-00-00	No	No	Current

PR